RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164085441
T1 Smith-Magenis Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164085441
RD 2020/03/31
AB A  syndrome  of  multiple  congenital  anomalies  characterized  by  midface  hypoplasia,  broad  face,  hearing  loss  (conductive  and/or  sensorineural),  congenital  heart  defect,  hypothyroidism,  severe  scoliosis,  brachydactyly,  and  decreased  pain  sensitivity  but  peripheral  neuropathy.  Severe  behavior  problems  (biting  and  head  banging)  and  sleep  disturbances.